Infliximab in primary Sjögren's syndrome: One‐year followup

Abstract
Objective To evaluate the safety and efficacy of a maintenance regimen of infliximab in patients with active primary Sjögren's syndrome (SS) over a 1‐year period. Methods This followup study included 10 of the 16 patients with primary SS who participated in a pilot study. Patients who continued to have symptoms received additional infusions of infliximab for 1 year. Results All patients completed the 1‐year followup for evaluation of efficacy. After 1 year, a statistically significant decrease in global and local disease manifestations was observed in all 10 patients. Treatment was generally well tolerated, with the main side effect being a mild, self‐limited infusion reaction. Conclusion Sustained improvement of active primary SS may be possible with infliximab treatment.
Funding Information
  • Fund for Medical Scientific Research (FRSM), Belgium (3.4551.01)